HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082587Generated: October 31, 2026
Carbon Dioxide → 1,4-Cyclohexane diisocyanate
https://huagongshe.com/reaction/2082587
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Diaminocyclohexane | HCID 18374 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,4-Cyclohexane diisocyanate | HCID 17367 | — |
Reaction Steps
Carbon dioxide was added subsurface to a dichloromethane (30 mL) solution containing 1,4-diaminocyclohexane (mixture of cis and trans, 0.02 mol 2.30 g) and triethylamine (0.12 mol, 12.0 g) at -10° C. (ice and salt bath) for 40 min at a pressure of 0 psig. The reaction mixture was transferred rapidly via cannula under carbon dioxide to the precooled solution of phosphorus oxychloride (0.04 mol, 6.2 g) in 30 mL dichloromethane. After stirring for ca. 30 min at -10° C. a white ppt formed. The ppt. was filtered off and the filtrate concentrated in vacuo. The residue was extracted with 3×30 mL diethyl ether. The ether layers were concentrated and the residue was distilled under vacuum (ca. 0.1-0.3 torr) collecting product, 1,4-cyclohexyl di-isocyanate, at 68°-78° C. (2.0 g, 60%) of 99% purity as judged by GC. IR (neat) 2266 cm-1. 1H NMR (CDCl3) δ 3.61 (br, 2H), 2.03-2.01 (m, 1H), 1.86-1.70 (m, 6H), 1.54-1.50 (m, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05189205 |
|---|
| Source dataset | uspto-grants-1993_02 |
|---|
| ORD ID | ord-ed0734d5b1b543fe8853c5e70f0cba26 |
|---|
| Source note | uspto-grants-1993_02 |
|---|